We evaluated the outcome of second allogeneic bone marrow transplantations
(BMTs) in 59 patients aged 1-57 years who relapsed after initial autologous
transplantation. Patients received a second transplantation for recurrent
acute myeloid leukemia (AML) (n = 24), acute lymphoblastic leukemia (ALL) (
n = 13), lymphoma (n = 18), multiple myeloma (n = 3), or chronic myelogenou
s leukemia (n = 1) from an HLA-matched related (n = 14), mismatched related
(n = 25), or matched unrelated (n = 20) donor. The probabilities of nonrel
apse mortality, relapse, and disease-free survival (DFS) 2 years after the
second BMT were 51%, 26%, and 23%, respectively. The 2-year DFS estimates f
or AE;IL, ALL, and lymphoma were 46%, 23%, and 0%. Univariate analysis demo
nstrated that superior DFS was associated with age less than or equal to 17
years at the time of the second transplantation remission before the secon
d transplantation, total-body irradiation-based preparative regimen for the
second transplantation, and the diagnosis of AML. These data demonstrate t
hat an allogeneic transplantation after a failed autologous transplantation
can result in disease-free survivors, especially in the young. The outcome
s after a second transplantation for patients aged >17 years and for those
with lymphoma were especially grim. These data suggest that pediatric patie
nts may be appropriate candidates for a second transplantation. In adults,
however, the use of an allogeneic transplantation as salvage therapy after
failure of the initial autologous transplantation is generally unsuccessful
. Alternative experimental strategies, such as low-dose nonmyeloablative al
logeneic minitransplantations should be considered.